Job Description

Oncology Research Pharmacist An established research center is seeking an experienced Oncology Research Pharmacist to support its expanding portfolio of oncology clinical trials. This position offers the opportunity to combine advanced pharmacy expertise with a purpose-driven mission to improve cancer care through research and innovation. As a key member of the clinical study team, you will collaborate with physicians, investigators, and research staff to ensure investigational medications are prepared, stored, and dispensed with the highest standards of accuracy and compliance. Responsibilities include reviewing trial protocols, overseeing drug accountability, maintaining study documentation, and supporting regulatory adherence across all phases of each study. Beyond technical execution, this position allows you to play a meaningful role in advancing oncology treatments that may redefine patient outcomes. The ideal candidate brings precision, teamwork, and a deep commitment to quality in a research-focused environment. Added Value: • Collaborate directly with physicians, investigators, and clinical teams • Participate in cutting-edge oncology research initiatives • Contribute to the advancement of investigational drug development • Maintain compliance with FDA, GCP, and institutional standards • Join a respected research center dedicated to innovation and patient care If you are a pharmacist who thrives in a research-driven environment and wants to make an impact on the future of cancer treatment, we would like to connect. Responsibilities: • Medication Management: Assess chemotherapy and oncology medications for clinical trial patients, ensuring proper dosing, administration, and side effect management. Oversee compounding and dispensing of chemotherapy meds in acute care settings. • Clinical Research Support : Provide pharmacological guidance for oncology clinical trials, ensuring compliance with GCP and regulatory guidelines. Clinical research experience is preferred but not required. • Pharmacovigilance : Monitor and report adverse events (AEs), serious adverse events (SAEs), adverse drug reactions (ADRs), medication errors, and drug interactions for investigational products in clinical trials. • Regulatory Compliance : Assist in protocol preparation, review, and adherence, including investigational drug management and regulatory inspections. • Collaboration : Work with oncology investigators, research coordinators, nurses, and other professionals to ensure optimal patient care and study outcomes, attending relevant clinical meetings. • Patient Education : Educate patients on medication regimens, risks, benefits, side effects, and management strategies within the context of clinical trials. • Data Analysis & Reporting : Contribute to data collection, analysis, and preparation of clinical study reports, publications, and regulatory submissions. • Professional Development : Stay up-to-date on oncology treatments, clinical trial methods, and pharmacological research through continuing education and relevant training. Qualifications: Education: • PharmD (Doctor of Pharmacy) from an accredited school of pharmacy. Licensure: • Active pharmacist license in California. Experience: • Minimum of 2 years of experience in oncology pharmacy practice. • Experience with investigational drugs, chemotherapy regimens, and oncology clinical research preferred. Certifications & Residency (preferred but not required): • Board Certification in Oncology Pharmacy (BCOP) is highly desirable (to be considered for the high end of the salary). • ASHP-accredited PGY-1 and PGY-2 residency in oncology or pain management is a plus. • Clinical Research Certification (ACRP or SOCRA) is a plus. Knowledge & Skills: • Strong knowledge of oncology pharmacotherapy, including chemotherapy, biologics, targeted therapies, and immunotherapy. • Strong communication, collaboration, organizational, and interpersonal skills. • Familiarity with clinical trial protocols, regulatory requirements, and ethical guidelines is preferred. • Proficiency with EHR/EMR systems and clinical trial management software is a plus. Personal Attributes: • Strong attention to detail with the ability to manage multiple projects simultaneously. • Ability to work independently and collaboratively within a research team. • Demonstrated commitment to patient safety and improving healthcare outcomes. Working Conditions: • Full-time, Monday to Friday, 9 am-5 pm with occasional travel (<10%) and overtime based on study needs. • Work is conducted in a clinical research setting with direct patient interaction in a hospital or outpatient clinic. • Must be currently located in Southern California. Salary listed reflects the maximum amount, dependent on experience (DOE) About Company: C-Clinical in Los Angeles drives clinical operations excellence across the pharmaceutical, biotechnology, and device sectors. Our chief concept is in guiding relationships and directing the government. We go by "love" in the principle: love your neighbor as yourself, and charity. C-Clinical was not an act of compulsion, but the care one would have for family. Bottom line - we created this company to do what we love to do: life-changing medical research, and to dedicate our time, talents, and resources to those who need them.

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Full time, Monday to Friday,

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